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NZ560350A - Thickening composition comprising xanthan gum particles which are coated with a potassium salt - Google Patents

Thickening composition comprising xanthan gum particles which are coated with a potassium salt

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Publication number
NZ560350A
NZ560350A NZ560350A NZ56035006A NZ560350A NZ 560350 A NZ560350 A NZ 560350A NZ 560350 A NZ560350 A NZ 560350A NZ 56035006 A NZ56035006 A NZ 56035006A NZ 560350 A NZ560350 A NZ 560350A
Authority
NZ
New Zealand
Prior art keywords
xanthan gum
potassium
gum particles
coated
thickening composition
Prior art date
Application number
NZ560350A
Inventor
Yoshinori Seko
Shuji Nishikawa
Tomohiro Kimura
Original Assignee
Taiyo Kagaku Kk
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taiyo Kagaku Kk filed Critical Taiyo Kagaku Kk
Publication of NZ560350A publication Critical patent/NZ560350A/en

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Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/20Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L27/00Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/60Salad dressings; Mayonnaise; Ketchup
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/20Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
    • A23L29/269Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of microbial origin, e.g. xanthan or dextran
    • A23L29/27Xanthan not combined with other microbial gums

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Dispersion Chemistry (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Medicinal Preparation (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

Disclosed is a method of producing a thickening composition which comprises: xanthan gum particles; and a potassium salt, in which the method is comprised of the steps of: a) coating the xanthan gum particles with the potassium salt to provide coated xanthan gum particles; b) subjecting the coated xanthan particles to a 30-second vibration in a 60-mesh JIS standard sieve having an inner diameter of 150 mm at a vibration width of 2 to 3 mm and 3600 counts/min; wherein less than 20% by weight of the coated xanthan gum particles crushed by vibration pass through the sieve; and the xanthan gum particles have a particle size finer than 60 mesh prior to step a). Also disclosed is a thickening composition which is prepared by the above method. Further disclosed is a food product, which comprises the above thickening composition.

Description

<div class="application article clearfix" id="description"> <p class="printTableText" lang="en">560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> DESCRIPTION <br><br> Thickening Composition Having Improved Viscosity-Producing Property <br><br> Technical Field <br><br>
[0001] <br><br> The invention relates to a thickening composition that can easily produce viscosity when added to a water-containing desired material, and particularly relates to a thickening composition with improved viscosity-producing properties that is suitable for use in thickening food products such as soft drinks, dips, sauces, dressings, soups, mousses, and jellies or suitable for use in producing viscosity with a small amount added to meals or the like for patients having difficulty in chewing or swallowing due to eating disorders. <br><br> Background Art <br><br>
[0002] <br><br> Xanthan gum is soluble in cold water, and the resulting solution exhibits strong pseudoplastic viscosity. The solution seems to form a weak network like a gel and therefore has excellent dispersing and emulsion-stabilizing properties for insoluble solids or fats and oils at relatively low viscosity. Xanthan gum also has good resistance to heat, acids, and freezing. For different types of high resistance, xanthan gum is used in various fields such as foods, cosmetics and pharmaceuticals. <br><br>
[0003] <br><br> In order to effectively use xanthan gum, it is first necessary to completely hydrate the xanthan gum. Only when it is completely hydrated, viscosity can be produced. When general users or the like use xanthan gum for food products and the like, xanthan gum powder <br><br> 1 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> can easily form so-called "aggregates" (a state in which only the surface of xanthan gum powder is dissolved and the inner part of the powder remains undissolved). The xanthan gum aggregates are insufficiently hydrated and tend to have a state in which its function cannot be performed. <br><br>
[0004] <br><br> When xanthan gum is hydrated, the viscosity development speed tends to increase with decreasing the particle size of xanthan gum and tends to decrease with increasing the particle size. Smaller-sized xanthan gum particles provide a larger surface area and tend to significantly form aggregates when dispersed in water, and thus require a dispersing or dissolving device or the like for complete hydration. Therefore, difficulties are associated with ensuring the dispersion and dissolution of xanthan gum. <br><br>
[0005] <br><br> Known conventional techniques for dispersing and dissolving xanthan gum in water include a technique in which xanthan gum is dispersed in ethanol and then dispersed and dissolved in the desired material such as water and a method in which xanthan gum is vigorously stirred with a stirring or dissolving device such as a disper such that it can be dissolved without forming aggregates. These methods, which are for industrial use, require a certain level of skill and are difficult to perform under domestic or other circumstances with no such equipment. <br><br>
[0006] <br><br> There is also disclosed a technique that includes using a water-soluble polysaccharide and an emulsifying agent for a binder solution and using the binder solution for granulation so that the solubility is improved (for example, see Patent Literature 1 below). In this method, however, aggregates can form depending on the feeding method, and the dissolution process is not always easy. There has been a demand for a composition that can <br><br> 2 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> be more easily dispersed and dissolved and quickly achieve the desired viscosity. <br><br>
[0007] <br><br> Patent Literature 1: Japanese Patent No. 3186737 <br><br> Disclosure of Invention <br><br> Objects to be Achieved by the Invention <br><br>
[0008] <br><br> Thus, there has been a demand for a composition that is prevented from forming aggregates like the conventional powder and can quickly achieve the desired viscosity. Such properties are strongly demanded particularly when xanthan gum is used to thicken care meals or training meals for persons with difficulty in chewing or swallowing. It is an object of the invention to provide a thickening composition that can quickly develop viscosity when added in a small amount to a water-containing desired material and can significantly reduce the user's working time, or at least to provide a useful alternative to known thickening compositions. <br><br> Description of the Invention [0008a] <br><br> Thus and in a first aspect, the present invention provides a thickening composition comprising: <br><br> xanthan gum particles; and a potassium salt, <br><br> wherein the xanthan gum particles are coated with the potassium salt to provide coated xanthan gum particles; <br><br> 3 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> the coated xanthan gum particles are subjected to a 30-second vibration in a 60-mesh JIS standard sieve having an inner diameter of 150 mm at a vibration width of 2 to 3 mm and 3600 counts/min; <br><br> 20% by weight or less of the coated xanthan gum particles crushed by vibration pass through the sieve; and xanthan gum particles prior to potassium salt coating have a particle size finer than 60 mesh. <br><br> In a second aspect, the present invention provides a food product, comprising the thickening composition as described above. <br><br> In a further aspect, the present invention provides a method of producing a thickening composition which comprises: <br><br> xanthan gum particles; and a potassium salt, <br><br> in which the method is comprised of the steps of: <br><br> a) coating the xanthan gum particles with the potassium salt to provide coated xanthan gum particles; <br><br> b) subjecting the coated xanthan particles to a 30-second vibration in a 60-mesh JIS standard sieve having an inner diameter of 150 mm at a vibration width of 2 to 3 mm and 3600 counts/min; <br><br> wherein less than 20% by weight of the coated xanthan gum particles crushed by vibration pass through the sieve; and the xanthan gum particles have a particle size finer than 60 mesh prior to step a). <br><br> 4 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> Means for Solving the Problems <br><br>
[0009] <br><br> In light of such circumstances, the inventors have made active investigations to improve the viscosity-producing properties and solubility of xanthan gum. As a result, the inventors have focused on the fact that when xanthan gum is dissolved, the solubility is reduced depending on the concentration of salts, and have found that when a potassium salt is allowed to bind to the surface of xanthan gum, for example, by spraying and drying a potassium chloride solution, only the surface of xanthan gum is modified to have reduced solubility so that the dispersibility of the xanthan gum in water can be significantly increased and that the xanthan gum dispersed in water can quickly develop viscosity. This necessarily requires the binding of a potassium salt to the xanthan gum surface. The process of simply mixing xanthan gum and potassium salt powder is not effective in improving the viscosity-producing properties. <br><br> Effects of the Invention <br><br>
[0010] <br><br> When a potassium salt is allowed to bind to the surface of xanthan gum powder, the water wettability of the xanthan gum surface is improved so that the dispersibility in water can be significantly improved and that the speed at which the peak viscosity is achieved can be significantly increased. <br><br> Best Mode for Carrying Out the Invention <br><br>
[0011] <br><br> Xanthan gum and a potassium salt permitted as food additives may be used in the <br><br> 5 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> invention. <br><br>
[0012] <br><br> In the invention, xanthan gum refers to a natural gum substance which is produced by purifying polysaccharides produced by the microbe Xanthomonas campestris fermentation of glucose and the like and accumulated extracellularly and preparing a powder of the polysaccharides. <br><br>
[0013] <br><br> In the invention, the potassium salt may be any potassium salt generally used for food products and may be at least one selected from the group consisting of potassium chloride, monopotassium citrate, tripotassium citrate, potassium hydrogen DL-tartrate, potassium hydrogen L-tartrate, potassium carbonate, tetrapotassium pyrophosphate, <br><br> potassium polyphosphate, potassium metaphosphate, tripotassium phosphate, dipotassium hydrogen phosphate, and potassium dihydrogen phosphate. In terms of further increasing the solubility, potassium chloride is preferred. <br><br>
[0014] <br><br> In the invention, the binding refers to the binding state of potassium salt particles on the surface of the xanthan gum particles and includes a state in which potassium salt particles bind, in the form of a crystal, to the surface of the xanthan gum particles, specifically, a state in which the potassium salt serves as a binder or a coating agent and binds to the xanthan gum surface. More specifically, the binding refers to a state in which the binding to the particles remains even when the particles are vibrated on a 60-mesh screen for 30 seconds. Fine powder that is formed by vibration-induced disintegration and passes through the 60-mesh screen is preferably at most 20% by weight, more preferably at most 15% by weight, still more preferably at most 10% by weight. In general, xanthan gum power and potassium chloride powder each have particle sizes of less than 60 mesh. Thus, if xanthan gum powder <br><br> 6 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> and potassium chloride powder are simply mixed and then the resulting powder mixture is sifted through the 60-mesh screen, 100% of the powder theoretically passes through the screen. <br><br>
[0015] <br><br> The binding may be achieved by any method. Examples of the method for the binding include a method that includes moisturizing xanthan gum and potassium salt particles to allow them to bind to each other and drying them and a method that includes uniformly spraying a potassium salt solution on xanthan gum powder and drying them. Preferably, a potassium salt solution is sprayed on xanthan gum and then subjected to fluidized drying, so that the potassium salt can be allowed to bind to the surface of the xanthan gum particles and that the binding of the potassium salt to the xanthan gum can be uniform. While the fluidized drying may be performed by any method, it is preferred that an aqueous 1 to 10% by weight solution of potassium chloride should be sprayed as a binder and then subjected to fluidized drying. With respect to the amount of the binding potassium salt, preferably 0.5 to 7 parts by weight of the potassium salt, more preferably 1 to 7 parts by weight of the potassium salt binds to 100 parts by weight of xanthan gum. An amount of more than 7 parts by weight is not preferred, because such an amount can lead to an increase in the hygroscopicity of the particles so that the development of viscosity can be slow. An amount of less than 0.5 parts by weight is not preferred, because such an amount of the potassium salt can provide a small amount of binding so that the development of viscosity cannot be accelerated. <br><br>
[0016] <br><br> In the invention, the peak viscosity refers to a viscosity value that is attained when xanthan gum is dispersed and dissolved in an ideal state. Specifically, when a certain amount of xanthan gum is dispersed and dissolved in a certain amount of water, it is observed <br><br> 7 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> that the viscosity tends to increase over time from immediately after the addition of the xanthan gum to the water, but the increase stops after a certain period of time, and the viscosity at that time is defined as the peak viscosity. For example, 1 g of xanthan gum is added to 99 g of water at 20°C and stirred for a certain time period (for 30 seconds, at 600 r/min), so that the viscosity starts to increase and is stabilized at a certain constant value after about 30 minutes. This viscosity is called the peak viscosity. When the potassium salt-binding xanthan gum is used according to the invention, the time period required to reach at least 90% of the peak viscosity can be at most 2 minutes after the addition, and thus the working time actually required for the user to prepare a thickener by hand stirring can be significantly reduced, as compared with a case where xanthan gum granules with no surface treatment are used, with which the time period required to reach at least 90% of the peak viscosity is at least 10 minutes. If the potassium salt-binding xanthan gum is compared with the xanthan gum granules with no surface treatment, rapid development of viscosity can be actually experienced because the former can be dispersed and dissolved without forming aggregates. <br><br>
[0017] <br><br> The thickening composition of the invention may have any composition, as long as it contains xanthan gum modified with the binding potassium salt. For example, however, at least one selected from guar gum, enzymatically decomposed guar gum, carrageenan, karaya gum, sodium CMC, sodium alginate, modified starch, and dextrin may also be used. While any type of dextrin may be used, DE (Dextrose Equivalent) is preferably from 6 to 30, more preferably from 6 to 25, in view of dispersibility. <br><br>
[0018] <br><br> The invention is more specifically described by showing the examples below, which are not intended to limit the scope of the invention. <br><br> 8 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br>
[0019] <br><br> Example 1 <br><br> Preparation of Binder Solution&gt; <br><br> Five g of potassium chloride was stirred and dissolved in 95 g of ion exchanged water at 50°C. <br><br>
[0020] <br><br> &lt;Spray Process&gt; <br><br> A hundred g of xanthan gum was maintained in a fluidized state, and 50 g of the potassium chloride solution was sprayed thereon. After the spray was completed, the resulting granules were fluidized and dried to give 94.3 g of a xanthan gum composition. A vessel with a volume of 100 ml was filled with the composition to the full level, and the weight of the deposited granules was measured. The weight of the granules was 41 g, and the bulk specific gravity was 0.41 g/ml. On a 60-mesh JIS standard screen with an inner diameter of 150 mm, 20 g of the resulting granules were vibrated for 30 seconds (OCTAGON 200 Model, Kabushiki Kaisha Iida-Seisakusho, a vibration width of 2 to 3 mm, 3600 times/minute) so that the degree of the particle binding was determined. As a result, out of the 20 g, 2.04 g of powder passed through the 60-mesh screen, and thus the content of xanthan gum and potassium chloride with a low binding degree was 10.2% by weight. It was demonstrated that the remaining 89.8% was in a biding state. The granules after the fluidized drying, the granules remaining on the 60-mesh screen, and the powder passing through the 60-mesh screen were each measured for potassium content per 100 g by atomic absorption spectrometry. As a result, the granules after the fluidized drying, the granules remaining on the 60-mesh screen, and the powder passing through the 60-mesh screen contained 1600 mg, 1600 mg, and 1600 mg of potassium, respectively, so that it was demonstrated that the potassium uniformly bound in the xanthan gum composition. <br><br> 9 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br>
[0021] <br><br> Comparative Example 1 <br><br> A comparative product was prepared similarly to Example 1, except that ion exchanged water was used in place of the potassium chloride solution. <br><br>
[0022] <br><br> &lt;Spray Process&gt; <br><br> A hundred g of xanthan gum and 2.5 g of potassium chloride powder (the same amount as in Example 1) were maintained in a fluidized state, and 50 g of ion exchanged water was sprayed thereon. After the spray was completed, the resulting granules were fluidized and dried to give 92 g of a xanthan gum composition. A vessel with a volume of 100 ml was filled with the composition to the full level, and the weight of the deposited granules was measured. The weight of the granules was 45 g, and the bulk specific gravity was 0.45 g/ml. The binding degree of 20g of the resulting granules was determined in the same manner as in Example 1. As a result, out of the 20 g, 4.18 g of powder passed through the 60-mesh screen, and the content of xanthan gum and potassium chloride with a low binding degree was 20.9% by weight. The granules after the fluidized drying, the granules remaining on the 60-mesh screen, and the powder passing through the 60-mesh screen were each measured for potassium content per 100 g by atomic absorption spectrometry in the same manner as in Example 1. As a result, the granules after the fluidized drying, the granules remaining on the 60-mesh screen, and the powder passing through the 60-mesh screen contained 1600 mg, 1400 mg, and 2500 mg of potassium, respectively. The potassium did not uniformly bound in the xanthan gum composition, and it was demonstrated that the weakly binding potassium chloride excessively passed through the 60-mesh screen. <br><br>
[0023] <br><br> Test Example 1 <br><br> 10 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br> Using a low-revolving disper (manufactured by Tokushu Kika Kogyo Co., Ltd.), 1 g of the granules obtained in Example 1 or Comparative Example 1 was added at a time to 99 g of ion exchanged water at 20°C with stirring at 600 r/min and stirred for 30 seconds. The mixture was then allowed to stand and measured for viscosity after 2, 5, 10, and 30 minutes with a B-type viscometer (manufactured by Tokyo Keiki, at a rotational speed of 12 r/min, with No. 3 rotor after 30 seconds). The viscosity measured after 30 minutes was normalized as 100%, and the results of the measurement were expressed as viscosity achievement rate percentages according to the formula: (measurement/ viscosity after 30 minutes) x 100. <br><br> With respect to Example 1 and Comparative Example 1, the results of the measurement are shown in Table 1, and the viscosity achievement rates are shown in Fig. 1. <br><br>
[0024] <br><br> Table 1 <br><br> Time (minutes) <br><br> 0 <br><br> 2 <br><br> 5 <br><br> 10 <br><br> 30 <br><br> Example 1 <br><br> 0 <br><br> 95.6 <br><br> 96.9 <br><br> 98 <br><br> 100 <br><br> Comparative Example 1 <br><br> 0 <br><br> 48 <br><br> 69 <br><br> 85 <br><br> 100 <br><br>
[0025] <br><br> In Example 1, the degree of binding between xanthan gum and potassium chloride was high, and the surface of the xanthan gum powder was modified at a high rate, so that the product had good dispersibility in water and was uniformly dispersed and dissolved in water and quickly developed viscosity without forming aggregates, even under weak stirring conditions. In Comparative Example 1, the binding degree of potassium chloride was low, and the surface of the xanthan gum powder was modified at a low rate, so that the product had poor dispersibility and formed aggregates under stirring and barely achieved the peak viscosity after 30 minutes. <br><br>
[0026] <br><br> 11 <br><br> 560350 <br><br> Received at IPONZ on 17 September 2010 <br><br> Test Example 2 <br><br> Example of Use in Food Product <br><br> The xanthan gum granules prepared in Example 1 were used to form a French dressing according to the formulation shown in Table 2. Different materials were simply mixed so that viscosity was developed and stabilized quickly after the mixing. Even after 30 <br><br> minutes, no change in viscosity was observed. <br><br>
[0027] <br><br> Table 2 <br><br> Example 1 <br><br> 0.5 <br><br> Vegetable Oil <br><br> 38 <br><br> Water <br><br> 37.5 <br><br> Granulated Sugar <br><br> 12 <br><br> Vinegar <br><br> 9 <br><br> Table Salt <br><br> 1 <br><br> Powdered Garlic <br><br> 1 <br><br> Powdered Mustard <br><br> 1 <br><br> Total <br><br> 100 <br><br> Industrial Applicability <br><br>
[0028] <br><br> The invention significantly reduces the time required to dissolve xanthan gum and also enables the dissolving process, which would otherwise require a skill in the prior art, at home or the like, without requiring any special technique or equipment. <br><br> Brief Description of Drawing <br><br>
[0029] <br><br> Fig. 1 is a graph showing viscosity achievement rates. <br><br> 12 <br><br> 560350 <br><br> Received at IPONZ on 31 August 2010 <br><br></p> </div>

Claims (1)

  1. <div class="application article clearfix printTableText" id="claims"> <p lang="en"> CLAIMS<br><br> A thickening composition, comprising:<br><br> xanthan gum particles; and a potassium salt,<br><br> wherein the xanthan gum particles are coated with the potassium salt to provide coated xanthan gum particles;<br><br> the coated xanthan gum particles are subjected to a 30-second vibration in a 60-mesh JIS standard sieve having an inner diameter of 150 mm at a vibration width of 2 to 3 mm and 3600 counts/min;<br><br> 20% by weight or less of the coated xanthan gum particles crushed by vibration pass through the sieve; and xanthan gum particles prior to potassium salt coating have a particle size finer than 60 mesh.<br><br> The thickening composition according to Claim 1, wherein the coated xanthan gum particles are prepared by a method comprising the steps of spraying a potassium salt solution onto xanthan gum particles, and thereafter fluidizing and drying the sprayed xanthan gum particles to produce the coated xanthan gum particles.<br><br> The thickening composition according to Claim 1 or 2, wherein the potassium salt is coated on the xanthan gum particles in an amount of 0.5 to 7 parts by weight to 100 parts by weight of the xanthan gum particles.<br><br> The thickening composition according to any one of Claims 1 to 3, wherein when the coated xanthan gum particles are added to ion-exchanged water in an amount of 1 part by weight based on 99 parts by weight of ion exchanged water at 20°C, the<br><br> 13<br><br> 560350<br><br> Received at IPONZ on 31 August 2010<br><br> xanthan gum is dispersed and dissolved without forming a lumpy mass, to reach at least 90% of a peak viscosity at 2 minutes after the addition.<br><br> 5. The thickening composition according to any one of Claims 1 to 4, wherein less than 15%) by weight of the coated xanthan gum particles crushed by vibration pass through the sieve.<br><br> 6. The thickening composition according to Claim 5, wherein less than 10% by weight of the coated xanthan gum particles crushed by vibration pass through the sieve.<br><br> 7. The thickening composition according to any one of Claims 1 to 6, wherein the potassium salt is one or more potassium salts selected from the group comprising potassium chloride, monopotassium citrate, tripotassium citrate, potassium DL-hydrogentartrate, potassium L-hydrogentartrate, potassium carbonate, tetrapotassium pyrophosphate, potassium polyphosphate, potassium metaphosphate, tripotassium phosphate, dipotassium hydrogenphosphate, and potassium dihydrogenphosphate.<br><br> 8. The thickening composition according to any one of Claims 1 to 7, wherein the thickening composition consists essentially of coated xanthan gum particles and the potassium salt is selected from the group comprising potassium chloride, monopotassium citrate, tripotassium citrate, potassium DL-hydrogentartrate, potassium L-hydrogentartrate, potassium carbonate, tetrapotassium pyrophosphate, potassium polyphosphate, potassium metaphosphate, tripotassium phosphate, dipotassium hydrogenphosphate, and potassium dihydrogenphosphate.<br><br> 9. A food product, comprising the thickening composition according to any one of Claims 1 to 8.<br><br> 10. A method of producing a thickening composition which comprises:<br><br> xanthan gum particles; and a potassium salt,<br><br> 14<br><br> 560350<br><br> Received at IPONZ on 31 August 2010<br><br> in which the method is comprised of the steps of:<br><br> a) coating the xanthan gum particles with the potassium salt to provide coated xanthan gum particles;<br><br> b) subjecting the coated xanthan particles to a 30-second vibration in a 60-mesh JIS standard sieve having an inner diameter of 150 mm at a vibration width of 2 to 3 mm and 3600 counts/min;<br><br> wherein less than 20% by weight of the coated xanthan gum particles crushed by vibration pass through the sieve; and the xanthan gum particles have a particle size finer than 60 mesh prior to step a).<br><br> 11. The method according to Claim 10, wherein step a) comprises the steps of:<br><br> i) spraying a potassium salt solution onto xanthan gum particles; and ii) fluidizing and drying the sprayed xanthan gum particles to produce the coated xanthan gum particles.<br><br> 12. The method according to Claim 10 or 11, wherein the potassium salt is coated on the xanthan gum particles in an amount of 0.5 to 7 parts by weight to 100 parts by weight of the xanthan gum particles.<br><br> 13. The method according to any one of Claims 10 to 12, wherein when the coated xanthan gum particles are added to ion-exchanged water in an amount of 1 part by weight based on 99 parts by weight of ion exchanged water at 20°C, the xanthan gum is dispersed and dissolved without forming a lumpy mass, to reach at least 90% of a peak viscosity at 2 minutes after the addition.<br><br> 14. The method according to any one of Claims 10 to 13, wherein less than 15% by weight of the coated xanthan gum particles crushed by vibration pass through the<br><br> 15<br><br> 560350<br><br> Received at IPONZ on 31 August 2010<br><br> sieve.<br><br> 15. The method according to Claim 14, wherein less than 10% by weight of the coated xanthan gum particles crushed by vibration pass through the sieve.<br><br> 16. The method according to any one of Claims 10 to 15, wherein the potassium salt is one or more potassium salts selected from the group comprising potassium chloride, monopotassium citrate, tripotassium citrate, potassium DL-hydrogentartrate, potassium L-hydrogentartrate, potassium carbonate, tetrapotassium pyrophosphate, potassium polyphosphate, potassium metaphosphate, tripotassium phosphate, dipotassium hydrogenphosphate, and potassium dihydrogenphosphate.<br><br> 17. The thickening composition according to Claim 1, substantially as herein described with reference to the Examples, but excluding the Comparative Examples.<br><br> 18. The thickening composition according to any one of Claims 1 to 8, substantially as herein described.<br><br> 19. The food product according to Claim 9 in which the thickening composition is substantially as herein described with reference to the Examples, but excluding the Comparative Examples.<br><br> 20. The food product according to Claim 9, substantially as herein described.<br><br> 21. The method according to Claim 10 in which the thickening composition is substantially as herein described with reference to the Examples, but excluding the Comparative Examples.<br><br> 22. The method according to any one of Claims 10 to 16, substantially as herein described.<br><br> 16<br><br> </p> </div>
NZ560350A 2005-03-11 2006-03-08 Thickening composition comprising xanthan gum particles which are coated with a potassium salt NZ560350A (en)

Applications Claiming Priority (2)

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JP2005069114 2005-03-11
PCT/JP2006/304436 WO2006095756A1 (en) 2005-03-11 2006-03-08 Thickening composition improved in viscosity manifestation

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NZ560350A true NZ560350A (en) 2010-10-29

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US (1) US7744942B2 (en)
EP (1) EP1867239B1 (en)
JP (2) JP4472699B2 (en)
KR (1) KR100840167B1 (en)
CN (1) CN101137295B (en)
AU (1) AU2006222583B2 (en)
BR (1) BRPI0609003B1 (en)
CA (1) CA2600380C (en)
DK (1) DK1867239T3 (en)
ES (1) ES2585355T3 (en)
NZ (1) NZ560350A (en)
RU (1) RU2434030C2 (en)
TW (1) TWI385181B (en)
WO (1) WO2006095756A1 (en)
ZA (1) ZA200706515B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9566303B2 (en) 2011-10-13 2017-02-14 Vidasym, Inc. Iron-fiber composition, preparation and uses thereof
US9796792B2 (en) 2013-03-08 2017-10-24 Vidasym, Inc. Metal ion-functional fiber component complex compositions, preparation and uses thereof

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007136083A1 (en) * 2006-05-24 2007-11-29 Meiji Dairies Corporation Thickener for liquid foods and method of producing the same
JP3930897B1 (en) * 2006-08-16 2007-06-13 太陽化学株式会社 Thickening composition with improved viscosity development
JP4909429B2 (en) 2010-04-27 2012-04-04 日清オイリオグループ株式会社 Thickener granulated product and method for producing the same
JP5913933B2 (en) 2011-11-30 2016-05-11 日澱化學株式会社 Thickening composition with improved dispersibility and metal salt-containing starch degradation product used therefor
KR102027625B1 (en) 2012-08-30 2019-10-01 닛신 오일리오그룹 가부시키가이샤 Granules and process for producing granules
JP5730376B2 (en) 2013-11-01 2015-06-10 松谷化学工業株式会社 Thickening composition and method for producing the same
JP5909791B1 (en) * 2015-02-12 2016-04-27 松谷化学工業株式会社 Xanthan gum granulated product and thickening composition
JP6766044B2 (en) * 2015-07-01 2020-10-07 株式会社明治 Splinter formation inhibitor
KR102004699B1 (en) * 2017-02-17 2019-07-29 대상라이프사이언스(주) High viscous composition used as food thickener with excellent dispersibility and rapid viscosity increase
JP7129191B2 (en) * 2018-03-28 2022-09-01 三栄源エフ・エフ・アイ株式会社 Method for producing modified xanthan gum and modified xanthan gum
CN120549217A (en) * 2019-07-12 2025-08-29 森永乳业株式会社 Composition for imparting thickening effect
CN111602805A (en) * 2020-06-01 2020-09-01 周益俊 A kind of edible instant thickener with high dispersibility and preparation method thereof
CN111793144A (en) * 2020-07-22 2020-10-20 内蒙古阜丰生物科技有限公司 Method for aligning fresh water viscosity and salt water viscosity of xanthan gum
CN112915069A (en) * 2021-03-03 2021-06-08 西安医学院 Fast-dispersing xanthan gum microcapsule and preparation method thereof

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3804951A (en) * 1971-10-01 1974-04-16 Miles Lab Egg extender composition and process therefor
JPS565839A (en) 1979-06-29 1981-01-21 Nippon Kayaku Co Ltd Water-soluble high polymer compound composition
JPS58198556A (en) 1982-05-14 1983-11-18 Katayama Chem Works Co Ltd Easily dispersible composition of water-soluble high-molecular material
US4487866A (en) * 1983-06-22 1984-12-11 Halliburton Company Method of improving the dispersibility of water soluble anionic polymers
US4729900A (en) * 1986-04-22 1988-03-08 Merck & Co., Inc. Foam-stabilized malt beverage
JPS6324865A (en) 1986-07-17 1988-02-02 Wakunaga Pharmaceut Co Ltd Granular paste and production thereof
JPH02299556A (en) * 1989-05-15 1990-12-11 Shikishima Boseki Kk Compounding material of food, production thereof and food containing same material
JP2820829B2 (en) 1991-03-07 1998-11-05 武田薬品工業株式会社 Nucleated powder and production method thereof
JPH05299556A (en) * 1992-04-20 1993-11-12 Shinko Electric Ind Co Ltd Package for electronic parts
GB9226391D0 (en) * 1992-12-18 1993-02-10 Cpc International Inc Xanthan gelling agents
JPH07322832A (en) 1994-05-31 1995-12-12 Kanebo Foods Ltd Production of powdery mix
US5728825A (en) * 1995-12-18 1998-03-17 Rhone-Poulenc Inc. Fast hydrating dust-free xanthan gum
JPH10108633A (en) * 1996-10-01 1998-04-28 Torigoe Seifun Kk Liquid food gelatinizing agent
CA2269598A1 (en) 1996-10-21 1998-04-30 Asahi Kasei Kogyo Kabushiki Kaisha Stabilizer for meat products and meat product composition
JP3822299B2 (en) * 1997-01-17 2006-09-13 扶桑化学工業株式会社 Water solubility promoter for poorly water soluble substances
JP3186737B2 (en) 1998-06-11 2001-07-11 不二製油株式会社 Method for producing water-soluble polysaccharide
CA2300456C (en) * 1999-03-12 2004-05-11 Pfizer Products Inc. Compositions comprising a potassium salt active ingredient, including oral compositions for reducing dental nerve and dentin sensitivity comprising a non-menthol flavoring
JP2000270792A (en) 1999-03-29 2000-10-03 Japan Organo Co Ltd Composition for thickening and gelation of food for aged people and production of food for aged
JP2001172395A (en) 1999-12-15 2001-06-26 Lion Corp Method for producing polymer solution
JP2001275584A (en) * 2000-03-29 2001-10-09 Ina Food Ind Co Ltd Powdery or granular thickener
FR2808705B1 (en) 2000-05-15 2003-01-17 Rhodia Chimie Sa POWDER COMPOSITION OF HYDROCOLLOIDS HAVING IMPROVED DISPERSABILITY IN AQUEOUS MEDIA AND PROCESS FOR THEIR PREPARATION
JP3795365B2 (en) 2001-09-28 2006-07-12 和光堂株式会社 Medication supplements
JP2003259838A (en) 2002-03-11 2003-09-16 Ndc:Kk Composition for water-soluble powdery food, drink, food and seasoning utilizing the same, and method for producing composition for water-soluble powdery food
RU2237420C2 (en) * 2002-08-27 2004-10-10 Открытое акционерное общество "Московский жировой комбинат" Mayonnaise
JP2004147567A (en) 2002-10-31 2004-05-27 Meiji Milk Prod Co Ltd Liquid food thickener and method for producing the same
PL1618149T3 (en) 2003-04-25 2007-07-31 Reckitt Benckiser Healthcare Thickenable compositions
JP4535779B2 (en) 2004-05-27 2010-09-01 太陽化学株式会社 Paste composition
JP4347248B2 (en) 2005-03-29 2009-10-21 森永乳業株式会社 Tromi composition
KR101758941B1 (en) 2009-08-31 2017-07-17 론자 리미티드 Process for the preparation of (1s,4r)-2-oxa-3-azabicyclo[2.2.1]hept-5-enes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9566303B2 (en) 2011-10-13 2017-02-14 Vidasym, Inc. Iron-fiber composition, preparation and uses thereof
US9796792B2 (en) 2013-03-08 2017-10-24 Vidasym, Inc. Metal ion-functional fiber component complex compositions, preparation and uses thereof

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EP1867239B1 (en) 2016-06-29
KR100840167B1 (en) 2008-06-23
EP1867239A4 (en) 2012-12-26
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BRPI0609003A2 (en) 2010-01-12
KR20070012331A (en) 2007-01-25
AU2006222583B2 (en) 2011-04-07
US20080280022A1 (en) 2008-11-13
ZA200706515B (en) 2008-09-25
TW200643032A (en) 2006-12-16
HK1114749A1 (en) 2008-11-14
JP4472699B2 (en) 2010-06-02
CA2600380A1 (en) 2006-09-14
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RU2434030C2 (en) 2011-11-20
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US7744942B2 (en) 2010-06-29
JP4800425B2 (en) 2011-10-26
WO2006095756A1 (en) 2006-09-14
EP1867239A1 (en) 2007-12-19
CA2600380C (en) 2011-06-28
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JP2010081943A (en) 2010-04-15

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